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FDA 510(k)

ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System

K-Number: K173981 · 2018-02-02

Decision Date2018-02-02
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is a medical device manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Group. It received FDA 510(k) clearance on 2018-02-02 under approval number K173981. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System?

ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-02-02. It is manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Group. The 510(k) number is K173981.

When was ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System approved by the FDA?

ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System received FDA 510(k) clearance on 2018-02-02, under approval number K173981.

What company makes ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System?

ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Group.

What is the FDA product code for ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System?

The FDA product code for ACUSON NX2 Diagnostic Ultrasound System, ACUSON NX2 Elite Diagnostic Ultrasound System is IYN.

Related Clinical Trials

Related PubMed Literature

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Official Source

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